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CAS

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ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2 is a peptide consisting of a sequence of amino acids including arginine, proline, lysine, glutamine, phenylalanine, glycine, leucine, and Nle (norleucine). This specific sequence forms a unique molecular structure that may confer biological functions and potential therapeutic applications.

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  • 57462-42-7 Structure

  • Basic information

    1. Product Name: ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2
    2. Synonyms: [NLE11]-SUBSTANCE P;ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2;H-ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2;substance P, NleNH2(11)-;Substance P, [Nle11];[Nle11]-Substance P;(Nle-NH211)-Substance P;[Norleucinamide11]substance P
    3. CAS NO:57462-42-7
    4. Molecular Formula: C64H100N18O13
    5. Molecular Weight: 1329.59
    6. EINECS: N/A
    7. Product Categories: Peptide
    8. Mol File: 57462-42-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: −20°C
    8. Solubility: N/A
    9. CAS DataBase Reference: ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2(CAS DataBase Reference)
    10. NIST Chemistry Reference: ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2(57462-42-7)
    11. EPA Substance Registry System: ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2(57462-42-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 57462-42-7(Hazardous Substances Data)

57462-42-7 Usage

Uses

Used in Biochemistry Research:
ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2 is used as a research tool for studying the structure-function relationships of peptides and their interactions with biological systems.
Used in Pharmaceutical Development:
This peptide is used as a potential therapeutic agent for various conditions, given its unique sequence and molecular structure that may offer specific biological activities.
Used in Biotechnology Applications:
ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2 is utilized in the development of novel biotechnological products, such as biosensors or drug delivery systems, due to its specific properties and potential for manipulation and optimization.
Used in the Food Industry:
In the food industry, this peptide may be used as a functional ingredient to enhance the nutritional value or to provide specific health benefits based on its amino acid composition and potential bioactivity.
Used in Cosmetics:
ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2 could be incorporated into cosmetic products for its potential skin health benefits, such as promoting collagen production or providing antioxidant effects, based on the properties of its constituent amino acids.

Check Digit Verification of cas no

The CAS Registry Mumber 57462-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,4,6 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 57462-42:
(7*5)+(6*7)+(5*4)+(4*6)+(3*2)+(2*4)+(1*2)=137
137 % 10 = 7
So 57462-42-7 is a valid CAS Registry Number.

57462-42-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ARG-PRO-LYS-PRO-GLN-GLN-PHE-PHE-GLY-LEU-NLE-NH2

1.2 Other means of identification

Product number -
Other names Substance P,[Nle11]

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:57462-42-7 SDS

57462-42-7Downstream Products

57462-42-7Relevant articles and documents

Synthesis of peptides by the solid-phase method. 7. Substance P and analogues

Fournier,Couture,Regoli,Gendreau,St-Pierre

, p. 64 - 68 (2007/10/02)

Substance P and 21 related peptides containing isosteric or isofunctional groups were prepared by the solid-phase method. After purification by gel filtration and ion-exchange chromatography, the compounds were characterized by thin-layer chromatography, paper electrophoresis, and amino acid and elemental analysis. The biological activities of the peptides were evaluated in vitro on the guinea pig ileum, the rabbit mesenteric vein, and the dog common carotid artery and in vivo on the rat blood pressure. It is shown that the replacement of some residues in the undecapeptide substance P causes variable losses of apparent affinity with a little or no change in the intrinsic activity. All the analogues used in the present study were found to be inactive as antagonists.

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